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MedTest DX, Inc. Lipid Controls

FDA UDI

Class I (US FDA UDI)

by Medtest DX

Identity

Trade Name
MedTest DX, Inc. Lipid Controls FDA UDI
Generic Name
Multiple lipid analyte IVD, control FDA UDI
Device Name
The Lipid Control set are assayed Lipid Controls produced from fresh human sera to monitor the accuracy and precision of quantitative lipid determinations of human sera specimens. 6 x 3 ml FDA UDI
Model / Reference
LIPC480 FDA UDI
Description
The Lipid Control set are assayed Lipid Controls produced from fresh human sera to monitor the accuracy and precision of quantitative lipid determinations of human sera specimens. 6 x 3 ml FDA UDI

Identifiers

Catalog Number
LIPC480 FDA UDI
Primary DI / UDI-DI
00817439021045 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple lipid analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

MedTest DX, Inc. Lipid Controls by Medtest DX — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtest DX

Sources (1)

  • FDA UDI 7ecbb105-e57c-4097-aaf4-ae87738ed837 37 fields · synced Jun 8, 2026